Asymmetric fluorine and chlorine side-chain engineered quinoxaline-based D-A copolymer for both fullerene and nonfullerene polymer solar cells

被引:3
|
作者
Zhou, Zhongxin [1 ]
Wu, Zhonglian [2 ]
Xu, Yongchuan [1 ]
Lu, Yingyi [1 ]
Yang, Jun [1 ]
Zhu, WeiGuo [1 ]
Liu, Yu [1 ]
机构
[1] Changzhou Univ, Jiangsu Collaborat Innovat Ctr Photovolta Sci & En, Natl Expt Demonstrat Ctr Mat Sci & Engn, Sch Mat Sci & Engn,Jiangsu Engn Lab Light Elect He, Changzhou 213164, Peoples R China
[2] Jiangsu Univ Technol, Sch Chem & Chem Engn, Changzhou 213001, Peoples R China
基金
美国国家科学基金会;
关键词
CONJUGATED POLYMERS; PERFORMANCE; MORPHOLOGY;
D O I
10.1039/d2py01122k
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this paper, one conjugated polymer, with asymmetric side chains of alkoxy-substituted difluorobenzene and alkoxy-substituted monochlorobenzene based on quinoxaline (Qx) as the electron acceptor unit, and alkylthiothiophene benzodithiophene (BDTTS) as the electron donor unit, namely PBDTTS-2FClQx, was synthesized and employed as an electron donor polymer with a compatible dual-acceptor strategy to fabricate ternary organic solar cells (OSCs). As a consequence, the optimized ternary OSC (PBDTTS-2FClQx:Y6:PC71BM = 1 : 0.9 : 0.1) exhibited a significantly enhanced PCE of 13.59% with simultaneously increased fundamental parameters, showing about 9.5% improvement compared to the control binary PBDTTS-2FClQx:Y6 (12.41%). Moreover, the optimal ternary device showed much better stability. The excellent results demonstrate that this Qx type copolymer bearing asymmetric side-chains could be a promising donor material for constructing efficient and stable OSCs.
引用
收藏
页码:728 / 736
页数:9
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